Diagnostic Tools of Waldenström's Macroglobulinemia - Best Possibilities for Non-invasive and Long-term Disease Monitoring
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F17%3AA1801QV2" target="_blank" >RIV/61988987:17110/17:A1801QV2 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.14735/amko20172S81" target="_blank" >http://dx.doi.org/10.14735/amko20172S81</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.14735/amko20172S81" target="_blank" >10.14735/amko20172S81</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Diagnostic Tools of Waldenström's Macroglobulinemia - Best Possibilities for Non-invasive and Long-term Disease Monitoring
Popis výsledku v původním jazyce
Waldenströms macroglobulinemia (WM) is a B-cell malignancy characterized by high levelof monoclonal immunoglobulin M (IgM) paraprotein in blood serum and associated with thebone marrow infi ltration by malignant cells with lymphoplasmacytic diff erentiation. WM remainsincurable advances in therapy. Most of WM cases are associated with a somatic pointmutation L265P in MYD88. Signifi cantly higher risk of progression from the IgM monoclonalgammopathy of undetermined signifi cance (IgM MGUS) to WM for patients with mutatedMYD88 gene suggests that this mutation is an early oncogenic event and plays a central role indevelopment of malignant clones. The second, most prevalent mutation in WM is found in theCXCR4 gene and is often associated with drug resistance and aggressive disease presentation.Therefore, detection of these mutations (MYD88L265P and CXCR4S338X) could be useful dia gnosticand prognostic tool for the patients with WM. While detection of these mutations in bonemarrow sample is common, the aim of our study was to compare sensitivity of detection ofmutation from diff erent cell fraction from peripheral blood and bone marrow. The results showpossibility to describe MYD88 and CXCR4 mutation status even from peripheral blood sample(sensitivity for MYD88L265P was 100%, for CXCR4S338X 91%), which signifi cantly facilitate materialcollection. Moreover, comparable detection sensitivity of these mutations in bone marrow andperipheral blood samples examined before and during the therapy off ers a promising tool formore routine dia gnostic and monitoring of disease progression.
Název v anglickém jazyce
Diagnostic Tools of Waldenström's Macroglobulinemia - Best Possibilities for Non-invasive and Long-term Disease Monitoring
Popis výsledku anglicky
Waldenströms macroglobulinemia (WM) is a B-cell malignancy characterized by high levelof monoclonal immunoglobulin M (IgM) paraprotein in blood serum and associated with thebone marrow infi ltration by malignant cells with lymphoplasmacytic diff erentiation. WM remainsincurable advances in therapy. Most of WM cases are associated with a somatic pointmutation L265P in MYD88. Signifi cantly higher risk of progression from the IgM monoclonalgammopathy of undetermined signifi cance (IgM MGUS) to WM for patients with mutatedMYD88 gene suggests that this mutation is an early oncogenic event and plays a central role indevelopment of malignant clones. The second, most prevalent mutation in WM is found in theCXCR4 gene and is often associated with drug resistance and aggressive disease presentation.Therefore, detection of these mutations (MYD88L265P and CXCR4S338X) could be useful dia gnosticand prognostic tool for the patients with WM. While detection of these mutations in bonemarrow sample is common, the aim of our study was to compare sensitivity of detection ofmutation from diff erent cell fraction from peripheral blood and bone marrow. The results showpossibility to describe MYD88 and CXCR4 mutation status even from peripheral blood sample(sensitivity for MYD88L265P was 100%, for CXCR4S338X 91%), which signifi cantly facilitate materialcollection. Moreover, comparable detection sensitivity of these mutations in bone marrow andperipheral blood samples examined before and during the therapy off ers a promising tool formore routine dia gnostic and monitoring of disease progression.
Klasifikace
Druh
J<sub>SC</sub> - Článek v periodiku v databázi SCOPUS
CEP obor
—
OECD FORD obor
30205 - Hematology
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Klinická onkologie
ISSN
1802-5307
e-ISSN
—
Svazek periodika
30
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
11
Strana od-do
81-91
Kód UT WoS článku
—
EID výsledku v databázi Scopus
2-s2.0-85029470000